Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QDQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0008654 | phospholipid biosynthetic process | 5 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 12 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 12 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 12 |
GO:0046486 | glycerolipid metabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004306 | ethanolamine-phosphate cytidylyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 12 |
GO:0070567 | cytidylyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.774 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.336 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.418 |
DEG_SCF_FBW7_1 | 553 | 560 | PF00400 | 0.634 |
DOC_CKS1_1 | 434 | 439 | PF01111 | 0.639 |
DOC_CKS1_1 | 533 | 538 | PF01111 | 0.642 |
DOC_CKS1_1 | 554 | 559 | PF01111 | 0.642 |
DOC_CYCLIN_RxL_1 | 44 | 52 | PF00134 | 0.617 |
DOC_MAPK_gen_1 | 335 | 345 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 391 | 399 | PF00069 | 0.559 |
DOC_MAPK_HePTP_8 | 239 | 251 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 223 | 230 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 306 | 313 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 341 | 348 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 463 | 472 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 520 | 528 | PF00069 | 0.459 |
DOC_MAPK_NFAT4_5 | 223 | 231 | PF00069 | 0.449 |
DOC_MAPK_NFAT4_5 | 341 | 349 | PF00069 | 0.484 |
DOC_MAPK_RevD_3 | 376 | 392 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 27 | 34 | PF00149 | 0.652 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.493 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.547 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.631 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.656 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.706 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.563 |
DOC_USP7_UBL2_3 | 585 | 589 | PF12436 | 0.633 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.639 |
LIG_14-3-3_CanoR_1 | 174 | 184 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 216 | 222 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 260 | 266 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 581 | 588 | PF00244 | 0.662 |
LIG_Actin_WH2_2 | 91 | 106 | PF00022 | 0.720 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.560 |
LIG_Clathr_ClatBox_1 | 378 | 382 | PF01394 | 0.344 |
LIG_EH1_1 | 288 | 296 | PF00400 | 0.449 |
LIG_EH1_1 | 417 | 425 | PF00400 | 0.523 |
LIG_eIF4E_1 | 340 | 346 | PF01652 | 0.581 |
LIG_eIF4E_1 | 418 | 424 | PF01652 | 0.550 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.481 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.242 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.614 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.395 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.547 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.542 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.363 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.476 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.612 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.750 |
LIG_IRF3_LxIS_1 | 184 | 190 | PF10401 | 0.451 |
LIG_LIR_Apic_2 | 480 | 484 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 531 | 536 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 538 | 544 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 163 | 170 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 286 | 297 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 362 | 370 | PF02991 | 0.330 |
LIG_LIR_LC3C_4 | 322 | 325 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.600 |
LIG_NRBOX | 181 | 187 | PF00104 | 0.363 |
LIG_NRBOX | 289 | 295 | PF00104 | 0.475 |
LIG_NRBOX | 401 | 407 | PF00104 | 0.637 |
LIG_NRBOX | 60 | 66 | PF00104 | 0.595 |
LIG_PDZ_Class_3 | 587 | 592 | PF00595 | 0.708 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.570 |
LIG_PTB_Apo_2 | 270 | 277 | PF02174 | 0.691 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.648 |
LIG_PTB_Phospho_1 | 270 | 276 | PF10480 | 0.693 |
LIG_PTB_Phospho_1 | 72 | 78 | PF10480 | 0.641 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.343 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.577 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.324 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.562 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.578 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.495 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.531 |
LIG_SH2_GRB2like | 521 | 524 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 533 | 537 | PF00017 | 0.561 |
LIG_SH2_SRC | 418 | 421 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.562 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.501 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.607 |
LIG_SH3_4 | 585 | 592 | PF00018 | 0.616 |
LIG_SH3_5 | 162 | 166 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 288 | 294 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 330 | 335 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 365 | 372 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 321 | 327 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 377 | 382 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 422 | 427 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 90 | 97 | PF11976 | 0.556 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.652 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.517 |
LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.473 |
LIG_TRFH_1 | 356 | 360 | PF08558 | 0.413 |
LIG_TYR_ITIM | 318 | 323 | PF00017 | 0.475 |
LIG_TYR_ITIM | 519 | 524 | PF00017 | 0.547 |
LIG_UBA3_1 | 308 | 315 | PF00899 | 0.441 |
LIG_UBA3_1 | 333 | 341 | PF00899 | 0.567 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.344 |
MOD_CDK_SPxK_1 | 433 | 439 | PF00069 | 0.638 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.635 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.573 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.321 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.275 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.487 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.677 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.363 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.507 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.461 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.634 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.543 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.561 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.464 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.330 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.384 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.466 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.573 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.528 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.516 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.568 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.611 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.442 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.541 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.709 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.395 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.336 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.518 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.649 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.521 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.545 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.469 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.588 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.467 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.725 |
MOD_PKB_1 | 203 | 211 | PF00069 | 0.607 |
MOD_PKB_1 | 567 | 575 | PF00069 | 0.606 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.765 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.438 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.343 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.520 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.578 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.709 |
MOD_Plk_2-3 | 584 | 590 | PF00069 | 0.722 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.772 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.349 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.335 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.328 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.354 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.348 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.286 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.529 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.491 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.578 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.565 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.540 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.630 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.638 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.476 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.640 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.636 |
MOD_SUMO_rev_2 | 574 | 583 | PF00179 | 0.728 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.637 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.579 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I259 | Leptomonas seymouri | 78% | 100% |
A0A0S4JNN5 | Bodo saltans | 47% | 100% |
A0A1X0P717 | Trypanosomatidae | 62% | 100% |
A0A3Q8IA23 | Leishmania donovani | 96% | 100% |
A0A422P0J5 | Trypanosoma rangeli | 60% | 100% |
A4H9L4 | Leishmania braziliensis | 89% | 100% |
A4HY04 | Leishmania infantum | 96% | 100% |
D0A5A2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9ARR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BEI8 | Trypanosoma cruzi | 59% | 100% |